Contribution of plasma membrane lipid domains to red blood cell (re)shaping

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作者
C. Leonard
L. Conrard
M. Guthmann
H. Pollet
M. Carquin
C. Vermylen
P. Gailly
P. Van Der Smissen
M. P. Mingeot-Leclercq
D. Tyteca
机构
[1] FACM Unit,
[2] Louvain Drug Research Institute & Université catholique de Louvain,undefined
[3] CELL Unit,undefined
[4] de Duve Institute & Université catholique de Louvain,undefined
[5] PEDI Unit,undefined
[6] Institut de Recherche expérimentale et clinique & Université catholique de Louvain,undefined
[7] CEMO Unit,undefined
[8] Institute of Neuroscience & Université catholique de Louvain,undefined
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摘要
Although lipid domains have been evidenced in several living cell plasma membranes, their roles remain largely unclear. We here investigated whether they could contribute to function-associated cell (re)shaping. To address this question, we used erythrocytes as cellular model since they (i) exhibit a specific biconcave shape, allowing for reversible deformation in blood circulation, which is lost by membrane vesiculation upon aging; and (ii) display at their outer plasma membrane leaflet two types of submicrometric domains differently enriched in cholesterol and sphingomyelin. We here reveal the specific association of cholesterol- and sphingomyelin-enriched domains with distinct curvature areas of the erythrocyte biconcave membrane. Upon erythrocyte deformation, cholesterol-enriched domains gathered in high curvature areas. In contrast, sphingomyelin-enriched domains increased in abundance upon calcium efflux during shape restoration. Upon erythrocyte storage at 4 °C (to mimick aging), lipid domains appeared as specific vesiculation sites. Altogether, our data indicate that lipid domains could contribute to erythrocyte function-associated (re)shaping.
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